Ocular characteristics and complications in patients with osteogenesis imperfecta: a systematic review

Author:

Treurniet Sanne1ORCID,Burger Pia1ORCID,Ghyczy Ebba A.E.2,Verbraak Frank D.2ORCID,Curro‐ Tafili Katie R.2,Micha Dimitra3,Bravenboer Nathalie4,Ralston Stuart H.5,Vries Ralph6,Moll Annette C.2ORCID,Eekhoff Elisabeth Marelise W.1

Affiliation:

1. Department of Internal Medicine, Section Endocrinology Amsterdam Bone Center Amsterdam University Medical Center Amsterdam The Netherlands

2. Department of Ophthalmology Amsterdam University Medical Center Amsterdam The Netherlands

3. Department of Clinical Genetics Amsterdam Movement Sciences Amsterdam University Medical Center Amsterdam The Netherlands

4. Department of Clinical Chemistry, Bone and Calcium Metabolism Lab Amsterdam University Medical Center Amsterdam The Netherlands

5. Centre for Genomic and Experimental Medicine MRC Institute of Genetics and Molecular Medicine University of Edinburgh Edinburgh UK

6. Medical library Vrije Universiteit Amsterdam The Netherlands

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Reference119 articles.

1. Compound heterozygous mutations in COL1A1 associated with an atypical form of type I osteogenesis imperfecta

2. Identification of a novel heterozygous mutation in exon 50 of the COL1A1 gene causing osteogenesis imperfecta;Aftab SAS;Endocrinol Diab Metab Case Rep,2013

3. Osteogenesis Imperfecta Type 1

4. Unilateral congenital third nerve palsy associated with osteogenesis imperfecta;Andalib D;Iran J Ophthalmol,2009

5. Retrospective Evaluation of Patients Diagnosed with Osteogenesis Imperfecta

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